Baxter is hiring for the position of Associate I, Quality Assurance in Ahmedabad, Gujarat. This is an excellent opportunity for pharma and life sciences professionals looking to build a career in Quality Assurance (QA), batch release, GMP compliance, and pharmaceutical manufacturing operations.
Baxter, a global healthcare leader, offers a purpose-driven work culture focused on improving patient outcomes. If you are experienced in batch disposition, deviation handling, and regulatory compliance, this role is highly relevant.
Job Details
- Job Title: Associate I, Quality Assurance
- Company: Baxter
- Location: Ahmedabad, Gujarat, India
- Job Type: Full-Time
- Job ID: JR – 197397
- Last Date to Apply: May 15, 2026
Key Responsibilities (Quality Assurance Pharma Role)
As part of the Quality Assurance team, you will handle critical QA functions in pharmaceutical manufacturing:
- Perform batch disposition after reviewing manufacturing, packing, and testing records
- Ensure compliance with SOPs, GMP guidelines, and regulatory standards
- Conduct impact assessments for change control proposals
- Investigate deviations, OOS (Out of Specification), and non-conformances
- Place affected batches on quality hold or quarantine when required
- Support root cause analysis and CAPA implementation
- Manage batch rejection and destruction procedures with documentation traceability
- Prepare Certificates of Conformity (CoC) and Manufacturing (CoM)
- Verify serialization and EMV data compliance before release
- Coordinate with warehouse and supply chain for batch release decisions
- Maintain daily QA batch tracking reports
- Support regulatory audits and authority queries
- Ensure continuous GMP compliance and quality system adherence
Required Qualifications
- Education: B.Pharm, M.Pharm, BSc, MSc (Life Sciences or related fields)
- Experience: 1โ3 years in Pharmaceutical Quality Assurance / QA / GMP environment
- Strong understanding of:
- Batch release process
- GMP guidelines
- Deviation & CAPA management
- Regulatory compliance
Preferred Skills
- Knowledge of pharma manufacturing processes
- Experience with QA documentation & audits
- Strong analytical and problem-solving skills
- Ability to handle regulatory inspections and compliance tasks
Salary & Benefits
- Estimated Salary: โน3.5 LPA โ โน6 LPA (based on industry standards)
- Work with a global healthcare leader
- Exposure to regulatory audits and GMP systems
- Career growth in pharmaceutical quality assurance domain
- Collaborative and purpose-driven work environment
Why Choose Baxter?
Baxter is known for its commitment to patient safety, innovation, and healthcare excellence. Working here means contributing to life-saving products while growing your expertise in pharma QA and compliance systems.
How to Apply
